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VEC Vectura Group Plc

164.80
0.00 (0.00%)
Last Updated: 01:00:00
Delayed by 15 minutes
Share Name Share Symbol Market Type Share ISIN Share Description
Vectura Group Plc LSE:VEC London Ordinary Share GB00BKM2MW97 ORD 0.0271P
  Price Change % Change Share Price Bid Price Offer Price High Price Low Price Open Price Shares Traded Last Trade
  0.00 0.00% 164.80 164.80 165.00 0.00 01:00:00
Industry Sector Turnover Profit EPS - Basic PE Ratio Market Cap
0 0 N/A 0

Vectura Group plc Launch of SeebriT Neohaler® in the US (1035U)

19/10/2017 1:17pm

UK Regulatory


Vectura (LSE:VEC)
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RNS Number : 1035U

Vectura Group plc

19 October 2017

Vectura Group plc

Launch of Seebri(TM) Neohaler(R) in the US

Chippenham, UK - 19 October 2017: Vectura Group plc (LSE: VEC) ("Vectura", "the Group"), an industry-leading device and formulation business for inhaled airways products, confirms that Sunovion Pharmaceuticals Inc. ("Sunovion"), the US licensee of the Group's partner Novartis AG ("Novartis"), has launched the twice-daily long acting muscarinic inhibitor (LAMA) Seebri(TM) Neohaler(R) (glycopyrrolate 15.6mcg), in the US.

Sunovion entered into an exclusive license agreement with Novartis for the US commercialisation rights to three of Novartis' COPD treatments, including Seebri(TM) Neohaler(R) and Utibron(TM) Neohaler(R) , on 21 December 2016 and in April 2017 Sunovion confirmed it had launched the dual long acting bronchodilator and muscarinic combination therapy (LABA-LAMA) Utibron(TM) Neohaler(R) , in the US.

Vectura is eligible to receive royalties from Novartis on net sales of the product as well as certain milestones based on global calendar year combined net sales of Utibron(TM) Neohaler(R) , Seebri(TM) Neohaler(R) , Ultibro(R) Breezhaler(R) and Seebri(R) Breezhaler(R) . The royalties earned upon net sales of Seebri(TM) Neohaler(R) are the same as those for Seebri(R) Breezhaler(R) .

James Ward-Lilley, Chief Executive Officer of Vectura:

"Following the launch of Utibron in April we are pleased with the confirmation of launch of Seebri in the US. Whilst the commercial priority for 2017 has been securing market access and product listings we remain confident that Sunovion will be effective in the commercialisation of these products given its strong US respiratory track record and look forward to this being reflected in strong revenue growth in the US for these two products."

Ultibro(R) Breezhaler(R) Seebri(R) Breezhaler(R) ,Utibron(TM) Neohaler(R) , Seebri(TM)Neohaler(R) are trademarks of Novartis AG.

- Ends -

Enquiries

 
Vectura Group plc                                                +44 (0)1249 667 700 
Andrew Derodra - Chief Financial Officer 
Fleur Wood - Director Communications 
Elizabeth Knowles - Director Investor Relations and Analysis 
 
 
Consilium Strategic Communications                               +44 (0)20 3709 5700 
Mary-Jane Elliott / Sue Stuart / Jessica Hodgson                  vectura@consilium-comms.com 
 
 

About Vectura

Vectura, a FTSE250 company listed on the London Stock Exchange (LSE: VEC), is an industry-leading device and formulation business for inhaled airways products offering a uniquely integrated inhaled drug delivery platform. With our extensive range of device and formulation technologies, integrated capabilities and collaborations, we are a leader in the development of inhalation products, increasing our ability to help patients suffering from respiratory diseases.

Vectura has eight inhaled, four non-inhaled and ten oral products marketed by partners with growing global royalty streams. The Group has a diverse portfolio of drugs in clinical development, including a number of novel and generic programmes which are partnered with several global pharmaceutical and biotechnology companies including Hikma, Novartis, Sandoz, Mundipharma, Kyorin, Baxter, GSK, UCB, Ablynx, Grifols, Bayer, Chiesi, Almirall, Janssen, Dynavax and Tianjin KingYork along with two wholly owned nebulised development programmes.

About Seebri(TM) Neohaler(R) (glycopyrrolate) Inhalation Powder

Seebri(TM) Neohaler(R) (glycopyrrolate) Inhalation Powder, 15.6 mcg twice daily, is a long-acting muscarinic antagonist (LAMA) approved in the U.S. for the long-term maintenance treatment of airflow obstruction in people with COPD, including chronic bronchitis and/or emphysema. SEEBRI NEOHALER is delivered by a dry powder inhaler (DPI), and its active ingredient, glycopyrrolate, has an established safety and efficacy profile. In clinical trials, SEEBRI NEOHALER improved lung function and showed reduced use of rescue medication and improvements in health-related quality of life, as measured by the St. George's Respiratory Questionnaire (SGRQ) total score, which is a composite of patient-reported symptoms, activities and impact on daily living.

The most common adverse reactions (>=1% and more common than placebo) reported in two 12-week clinical trials with SEEBRI NEOHALER (and placebo) were: upper respiratory tract infection, 3.4% (2.3%); nasopharyngitis, 2.1% (1.9%); urinary tract infection, 1.4% (1.3%); sinusitis, 1.4% (0.7%); oropharyngeal pain, 1.8% (1.2%).

About Long-Acting Muscarinic Antagonists (LAMAs)

A long-acting muscarinic antagonist (LAMA) is a type of long-acting bronchodilator, along with long-acting beta(2) agonists (LABAs). According to the GOLD report, these are currently the first-line standard of care maintenance therapy for symptomatic patients with COPD, and help the muscles around the airways in lungs stay relaxed to prevent symptoms such as wheezing, coughing, chest tightness and shortness of breath.[i] LAMAs and LABAs are widely used and

important therapeutic approaches for people with COPD.

About COPD

Chronic obstructive pulmonary disease (COPD) is a common, preventable and treatable disease that is characterized by persistent respiratory symptoms and airflow limitation that is due to airway and/or lung abnormalities usually caused by significant exposure to toxic particles or gases. The main risk factor for COPD is tobacco smoking, but other environmental exposures may contribute.(i) Approximately 15.7 million adults in the U.S. report that they have been diagnosed with COPD.[ii] It is estimated that several million more adults have undiagnosed COPD.[iii] COPD is responsible

for over 120,000 deaths per year, making it the third leading cause of death in the U.S.(iii) COPD develops slowly and the symptoms often worsen over time, potentially limiting the ability to perform routine activities.(ii) Symptoms of COPD include coughing, wheezing, shortness of breath, excess production of mucus in the lungs, the inability to breathe deeply and the feeling of being unable to breathe.[iv] The symptoms of COPD can be most severe during the night and early morning.[v] Morning symptoms can be associated with limitation of activities during the day, impaired health status and increased risk of exacerbation.[vi] Night-time symptoms disturb sleep, reduce sleep quality and, in the long term, may be associated with development or worsening of cardiovascular diseases, cognition, depression and increased mortality.[vii]

Forward-looking statements

This press release contains forward-looking statements, including statements about the discovery, development and commercialisation of products. Various risks may cause Vectura's actual results to differ materially from those expressed or implied by the forward-looking statements, including: adverse results in clinical development programmes; failure to obtain patent protection for inventions; commercial limitations imposed by patents owned or controlled by third parties; dependence upon strategic alliance partners to develop and commercialise products and services; difficulties or delays in obtaining regulatory approvals to market products and services resulting from development efforts; the requirement for substantial funding to conduct research and development and to expand commercialisation activities; and product initiatives by competitors. As a result of these factors, prospective investors are cautioned not to rely on any forward-looking statements. We disclaim any intention or obligation to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise.

[i] GOLD Guidelines 2017. http://www.goldcopd.org/guidelines-global-strategy-for-diagnosis-management.html. Accessed: March 16, 2017.

[ii] MMWR: Morbidity and Mortality Weekly Report. Employment and Activity Limitations Among Adults with Chronic Obstructive Pulmonary Disease - United States, 2013. March 27,

2015; 64(11). Available at http://www.cdc.gov/mmwr/

[iii] National Heart, Lung, and Blood Institute. "What is COPD?" Available at: http://www.nhlbi.nih.gov/health/educational/copd/what-is-copd/index.htm. Accessed: March 2, 2016

[iv] National Heart, Lung and Blood Institute. (2013). What Are the Signs and Symptoms of COPD? Retrieved from https://www.nhlbi.nih.gov/health/health-topics/topics/copd/signs.

[v] Partridge MR, Karlsson N, Small IR. Patient insight into the impact of chronic obstructive pulmonary disease in the morning: an internet survey. Curr Med Res Opin. 2009;25:2043-8.

[vi] Roche N, Small M, Broomfield S, Higgins V, Pollard R. Real world COPD: association of morning symptoms with clinical and patient reported outcomes. COPD. 2013;10:679-86.

[vii] Agusti A, Hedner J, Marin JM, Barbé F, Cazzola M, Rennard S. Night-time symptoms: a forgotten dimension of COPD. Eur Respir Rev. 2011;20:183-94.

This information is provided by RNS

The company news service from the London Stock Exchange

END

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(END) Dow Jones Newswires

October 19, 2017 08:17 ET (12:17 GMT)

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